Canonical Allele Identifier: CA1978008758
Gene: SLC22A8 HGNC NCBI

Linked Data

dbSNP Id: rs190860044

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62991201G>A , CM000673.2:g.62991201G>A GRCh38
NC_000011.9:g.62758673G>A , CM000673.1:g.62758673G>A GRCh37
NC_000011.8:g.62515249G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000539841.1:n.5531C>T